Transfer guard systems and methods

ABSTRACT

A transfer guard may provide a fluid path from a vial to a reservoir containing a plunger head connected to a plunger arm operatively engagable with a handle that at least partially covers a casing configured to allow the handle to operatively engage the plunger arm to move the plunger head to transfer fluidic media from the vial to the reservoir. 
     A support structure may have a chamber, a first adapter for mating with a vial containing fluidic media, and a second adapter for mating with a reservoir containing a plunger head moveable within the reservoir. A first needle may provide a fluid path from the vial to the reservoir and a second needle may connect the vial and the chamber containing an air flow control mechanism for allowing air to flow in one direction.

CROSS-REFERENCE TO RELATED PATENT APPLICATIONS

This application is a Divisional of U.S. application Ser. No.12/537,579, filed Aug. 7, 2009, incorporated herein by reference in itsentirety.

BACKGROUND

1. Field of the Invention

Embodiments of the present invention generally relate to systems andmethods with reservoirs, and, in specific embodiments, to systems andmethods for assisted filling of reservoirs.

2. Related Art

According to modern medical techniques, certain chronic diseases may betreated by delivering a medication or other substance to the body of apatient. For example, diabetes is a chronic disease that is commonlytreated by delivering defined amounts of insulin to a patient atappropriate times. Traditionally, manually operated syringes and insulinpens have been employed for delivering insulin to a patient. Morerecently, modern systems have been designed to include programmablepumps for delivering controlled amounts of medication to a patient.

Pump type delivery devices have been configured in external devices,which connect to a patient, and have been configured in implantabledevices, which are implanted inside of the body of a patient. Externalpump type delivery devices include devices designed for use in astationary location, such as a hospital, a clinic, or the like, andfurther include devices configured for ambulatory or portable use, suchas devices designed to be carried by a patient, or the like. Externalpump-type delivery devices may contain reservoirs of fluidic media, suchas, but is not limited to, insulin.

External pump-type delivery devices may be connected in fluid flowcommunication to a patient or user-patient, for example, throughsuitable hollow tubing. The hollow tubing may be connected to a hollowneedle that is designed to pierce the skin of the patient and to deliverfluidic media there through. Alternatively, the hollow tubing may beconnected directly to the patient as through a cannula, or the like.

Examples of some external pump type delivery devices are described inU.S. patent application Ser. No. 11/211,095, filed Aug. 23, 2005, titled“Infusion Device And Method With Disposable Portion” and Published PCTApplication WO 01/70307 (PCT/US01/09139) titled “Exchangeable ElectronicCards For Infusion Devices” (each of which is owned by the assignee ofthe present invention), Published PCT Application WO 04/030716(PCT/US2003/028769) titled “Components And Methods For Patient InfusionDevice,” Published PCT Application WO 04/030717 (PCT/US2003/029019)titled “Dispenser Components And Methods For Infusion Device,” U.S.Patent Application Publication No. 2005/0065760 titled “Method ForAdvising Patients Concerning Doses Of Insulin,” and U.S. Pat. No.6,589,229 titled “Wearable Self-Contained Drug Infusion Device,” each ofwhich is incorporated herein by reference in its entirety.

External pump-type delivery devices may be connected in fluid-flowcommunication to a patient-user, for example, through suitable hollowtubing. The hollow tubing may be connected to a hollow needle that isdesigned to pierce the patient-user's skin and deliver an infusionmedium to the patient-user. Alternatively, the hollow tubing may beconnected directly to the patient-user as or through a cannula or set ofmicro-needles.

In contexts in which the hollow tubing is connected to the patient-userthrough a hollow needle that pierces skin of the user-patient, a manualinsertion of the needle into the patient-user can be somewhat traumaticto the user-patient. Accordingly, insertion mechanisms have been made toassist the insertion of a needle into the user-patient, whereby a needleis forced by a spring to move quickly from a retracted position into anextended position. As the needle is moved into the extended position,the needle is quickly forced through the skin of the user-patient in asingle, relatively abrupt motion that can be less traumatic to certainuser-patients as compared to a slower, manual insertion of a needle.While a quick thrust of the needle into the skin of the user-patient maybe less traumatic to some user-patients than a manual insertion, it isbelieved that, in some contexts, some user-patients may feel less traumaif the needle is moved a very slow, steady pace.

Examples of insertion mechanisms that may be used with and may be builtinto a delivery device are described in: U.S. patent application Ser.No. 11/645,435, filed Dec. 26, 2006, titled “Infusion Medium Deliverysystem, Device And Method With Needle Inserter And Needle InserterDevice And Method,”; and U.S. patent application Ser. No. 11/211,095,filed Aug. 23, 2005, titled “Infusion Device And Method With DisposablePortion” (each of which is assigned to the assignee of the presentinvention), each of which is incorporated herein by reference in itsentirety. Other examples of insertion tools are described in U.S. PatentApplication Publication No. 2002/0022855, titled “Insertion Device ForAn Insertion Set And Method Of Using The Same” (assigned to the assigneeof the present invention), which is incorporated herein by reference inits entirety. Other examples of needle/cannula insertion tools that maybe used (or modified for use) to insert a needle and/or cannula, aredescribed in, for example U.S. patent application Ser. No. 10/389,132filed Mar. 14, 2003, and entitled “Auto Insertion Device For SilhouetteOr Similar Products,” and/or U.S. patent application Ser. No. 10/314,653filed Dec. 9, 2002, and entitled “Insertion Device For Insertion Set andMethod of Using the Same,” both of which are incorporated herein byreference in their entirety.

Pump-type delivery devices can allow accurate doses of insulin to becalculated and delivered automatically to a patient-user at any timeduring the day or night. Furthermore, when used in conjunction withglucose sensors or monitors, insulin pumps may be automaticallycontrolled to provide appropriate doses of infusion medium atappropriate times of need, based on sensed or monitored levels of bloodglucose.

Pump-type delivery devices have become an important aspect of modernmedical treatments of various types of medical conditions, such asdiabetes. As pump technologies improve and as doctors and patient-usersbecome more familiar with such devices, the popularity of externalmedical infusion pump treatment increases and is expected to increasesubstantially over the next decade.

SUMMARY OF THE DISCLOSURE

A system for transferring fluidic media may include, but is not limitedto, a transfer guard, a handle, and a casing. The transfer guard may befor providing a fluid path from a vial to a reservoir. The handle may beconfigured to be operatively engagable to a plunger arm connected to aplunger head arranged for movement in an axial direction of thereservoir. The casing may be configured to allow the plunger arm to movein the axial direction relative to the reservoir to move the plungerhead in the axial direction within the reservoir. The handle may beconfigured to cover at least a portion of the casing The transfer guardand the handle may be configured such that fluidic media is transferredfrom the vial to the reservoir in a case where the handle is operativelyengaged to the plunger arm and the handle is moved relative to the axialdirection relative to the reservoir.

In various embodiments, the casing may have an opening for allowing thehandle to operatively engage the plunger arm. In various embodiments,the handle may include an engagement portion configured for pivotalmovement to operatively engage and disengage the plunger arm. In someembodiments, the handle may include a slide adapted to cause the pivotalmovement of the engagement portion to operatively engage and disengagethe plunger arm. In further embodiments, the slide may be adapted tomove at least between a first position and a second position. Theengagement portion may be configured to engage the plunger arm when theslide is moved to the first position. The engagement portion may beconfigured to disengage the plunger arm when the slide is moved to thesecond position.

In some embodiments, the engagement portion may have an extension. Theplunger arm may have an aperture for receiving the extension when theengagement portion of the handle operatively engages the plunger arm. Infurther embodiments, the extension of the engagement portion may be forextending through an opening in the casing to operatively engage theaperture in the plunger arm and for allowing the extension of theengagement portion to move along the opening as the plunger arm is movedby the handle.

In various embodiments, the transfer guard may have an end for matingwith the reservoir. The end may comprise a body configured to envelopthe reservoir. In some embodiments, the body may be adapted to allowfluidic media in the reservoir to be viewable through the body in a casewhere the reservoir is connected to the end of the transfer guard andthe reservoir contains fluidic media. In further embodiments, the bodymay have an opening for allowing fluidic media in the reservoir to beviewable and for allowing a user-patient to provide further support tothe reservoir during use of the system. In some embodiments, the bodymay have one or more fill lines for measuring a volume of fluidic mediain the reservoir.

In various embodiments, the transfer guard may have a chamber. Thetransfer guard may include, but is not limited to, a first needle, asecond needle, and an air flow control mechanism. The first needle maybe for connecting the interior volume of the vial to the interior volumeof the reservoir to provide a fluid flow path from the interior volumeof the vial to the interior volume of the reservoir. The second needlemay be for connecting the chamber and the interior volume of the vial.The air flow control mechanism may be arranged within the chamber andconfigured to allow air to flow in one direction in a case where thesecond needle connects the chamber and the vial and the plunger head ismoved within the reservoir to transfer fluidic media from the interiorvolume of the vial to the interior volume of the reservoir.

In some embodiments, the air flow control mechanism may be configured toallow the chamber to communicate with atmosphere to equalize pressurerelative to atmosphere in the interior volume of the vial in a casewhere the second needle connects the chamber and the vial and theplunger head is moved within the reservoir to transfer fluidic mediafrom the interior volume of the vial to the interior volume of thereservoir. In some embodiments, the air flow control mechanism maycomprise a membrane configured to allow air to flow in one direction. Insome embodiments, the air flow control mechanism may comprise a valve.In further embodiments, the valve may comprise at least one of anumbrella valve and a duckbill valve configured to allow air to flow inone direction.

A method of making a system for transferring fluidic media may include,but is not limited to, any one of or combination of: (i) providing atransfer guard for providing a fluid path from a vial to a reservoir;(ii) configuring a handle to be operatively engagable to a plunger armconnected to a plunger head arranged for movement in an axial directionof the reservoir; (iii) configuring a casing to allow the plunger arm tomove in the axial direction relative to the reservoir to move theplunger head in the axial direction within the reservoir; (iv)configuring the handle to cover at least a portion of the casing; and(v) configuring the transfer guard and the handle such that fluidicmedia is transferred from the vial to the reservoir in a case where thehandle is operatively engaged to the plunger arm and the handle is movedin the axial direction relative to the reservoir.

A system for transferring fluidic media may include, but is not limitedto, a support structure, a first needle, a second needle, and an airflow control mechanism. The support structure may have a chamber. Thesupport structure may include, but is not limited to a first adapter anda second adapter. The first adapter may be adapted to be mated to a vialhaving an interior volume containing fluidic media. The second adaptermay be adapted to be mated to a reservoir having an interior volume forcontaining fluidic media and a plunger head arranged for movement withinthe reservoir.

The first needle may be for connecting the interior volume of the vialto the interior volume of the reservoir to provide a fluid flow pathfrom the interior volume of the vial to the interior volume of thereservoir. The second needle may be for connecting the chamber and theinterior volume of the vial. The air flow control mechanism may bearranged within the chamber and configured to allow air to flow in onedirection in a case where the second needle connects the chamber and thevial and the plunger head is moved within the reservoir to transferfluidic media from the interior volume of the vial to the interiorvolume of the reservoir.

In various embodiments, at least a portion of the first needle may beconcentrically arranged within at least a portion of the second needle.In some embodiments, the first needle and the second needle may share acommon axis. In some embodiments, an axis of the first needle and anaxis of the second needle may be parallel to each other. The axis of thefirst needle may be offset from the axis of the second needle.

In various embodiments, the air flow control mechanism may be adapted toallow the chamber to communicate with atmosphere to equalize pressurerelative to atmosphere in the interior volume of the vial in a casewhere the second needle connects the chamber and the vial and theplunger head is moved within the reservoir to transfer fluidic mediafrom the interior volume of the vial to the interior volume of thereservoir. In various embodiments, the air flow control mechanism maycomprise a membrane. In various embodiments, the air flow controlmechanism may comprise a valve. In some embodiments, the air flowcontrol mechanism may comprise at least one of an umbrella valve and aduckbill valve. In some embodiments, the valve may be moveable at leastbetween a first position and a second position. The chamber may be forcommunicating with atmosphere in a case where the valve is in the secondposition and the fluid flow path is established.

In various embodiments, the second adapter may comprise a bodyconfigured to envelop the reservoir. In some embodiments, the body maybe adapted to allow fluidic media in the reservoir to be viewablethrough the body in a case where the reservoir is connected to thesecond adapter and the reservoir contains fluidic media. In furtherembodiments, the body may have an opening for allowing fluidic media inthe reservoir to be viewable and for allowing a user-patient to providefurther support to the reservoir during use of the system. In someembodiments, the body may have one or more fill lines for measuring avolume of fluidic media in the reservoir.

A method of making a system for transferring fluidic media may includebut is not limited to, any one of or combination of: (i) supporting asupport structure having a chamber, the support structure comprising: afirst adapter adapted to be mated to a vial having an interior volumecontaining fluidic media; and a second adapter adapted to be mated to areservoir having an interior volume for containing fluidic media and aplunger head arranged for movement within the reservoir; (ii) connectingthe interior volume of the vial to the interior volume of the reservoirto provide a fluid flow path from the interior volume of the vial to theinterior volume of the reservoir with a first needle; (iii) connectingthe chamber and the interior volume of the vial with a second needle;and (iv) arranging an air flow control mechanism within the chamber andconfiguring the air flow control mechanism to allow air to flow in onedirection in a case where the second needle connects the chamber and thevial and the plunger head is moved within the reservoir to transferfluidic media from the interior volume of the vial to the interiorvolume of the reservoir.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates a generalized representation of a system inaccordance with an embodiment of the present invention;

FIG. 2 illustrates an example of a system in accordance with anembodiment of the present invention;

FIG. 3 illustrates an example of a delivery device in accordance with anembodiment of the present invention;

FIG. 4 illustrates a delivery device in accordance with an embodiment ofthe present invention;

FIG. 5A illustrates a durable portion of a delivery device in accordancewith an embodiment of the present invention;

FIG. 5B illustrates a section view of a durable portion of a deliverydevice in accordance with an embodiment of the present invention;

FIG. 5C illustrates a section view of a durable portion of a deliverydevice in accordance with an embodiment of the present invention;

FIG. 6A illustrates a disposable portion of a delivery device inaccordance with an embodiment of the present invention;

FIG. 6B illustrates a section view of a disposable portion of a deliverydevice in accordance with an embodiment of the present invention;

FIG. 6C illustrates a section view of a disposable portion of a deliverydevice in accordance with an embodiment of the present invention;

FIG. 7 is a cross-section of a portion of a medical device in accordancewith an embodiment of the present invention;

FIG. 8A is a cross-section of a portion of a medical device inaccordance with an embodiment of the present invention;

FIG. 8B is a cross-section of a portion of a medical device inaccordance with an embodiment of the present invention;

FIG. 8C is a cross-section of a portion of a medical device inaccordance with an embodiment of the present invention;

FIG. 9 illustrates a medical device in accordance with an embodiment ofthe present invention;

FIG. 10 illustrates a portion of a medical device in accordance with anembodiment of the present invention;

FIG. 11 illustrates a portion of a medical device in accordance with anembodiment of the present invention;

FIG. 12 illustrates a portion of a medical device in accordance with anembodiment of the present invention;

FIG. 13 is a cross-section of a portion of a medical device inaccordance with an embodiment of the present invention;

FIG. 14A is a cross-section of a portion of a medical device inaccordance with an embodiment of the present invention;

FIG. 14B is a cross-section of a portion of a medical device inaccordance with an embodiment of the present invention;

FIG. 14C is a cross-section of a portion of a medical device inaccordance with an embodiment of the present invention;

FIG. 15 illustrates a flowchart for using a medical device in accordancewith an embodiment of the present invention;

FIG. 16A illustrates a portion of a medical device in accordance with anembodiment of the present invention;

FIG. 16B illustrates a portion of a medical device in accordance with anembodiment of the present invention; and

FIG. 17 is a cross-section of a portion of a medical device inaccordance with an embodiment of the present invention.

DETAILED DESCRIPTION

FIG. 1 illustrates a generalized representation of a system 10 inaccordance with an embodiment of the present invention. The system 10includes a delivery device 12. The system 10 may further include asensing device 14, a command control device (CCD) 16, and a computer 18.In various embodiments, the delivery device 12 and the sensing device 14may be secured at desired locations on the body 5 of a patient oruser-patient 7. The locations at which the delivery device 12 and thesensing device 14 are secured to the body 5 of the user-patient 7 inFIG. 1 are provided only as representative, non-limiting, examples.

The system 10, the delivery device 12, the sensing device 14, the CCD16, and computer 18 may be similar to those described in the followingU.S. patent applications that were assigned to the assignee of thepresent invention, where each of following patent applications isincorporated herein by reference in its entirety: (i) U.S. patentapplication Ser. No. 11/211,095, filed Aug. 23, 2005, “Infusion DeviceAnd Method With Disposable Portion”; (ii) U.S. patent application Ser.No. 11/515,225, filed Sep. 1, 2006, “Infusion Medium Delivery Device AndMethod With Drive Device For Driving Plunger In Reservoir”; (iii) U.S.patent application Ser. No. 11/588,875, filed Oct. 27, 2006, “SystemsAnd Methods Allowing For Reservoir Filling And Infusion MediumDelivery”; (iv) U.S. patent application Ser. No. 11/588,832, filed Oct.27, 2006, “Infusion Medium Delivery Device And Method With Drive DeviceFor Driving Plunger In Reservoir”; (v) U.S. patent application Ser. No.11/588,847, filed Oct. 27, 2006, “Infusion Medium Delivery Device AndMethod With Compressible Or Curved Reservoir Or Conduit”; (vi) U.S.patent application Ser. No. 11/589,323, filed Oct. 27, 2006, “InfusionPumps And Methods And Delivery Devices And Methods With Same”; (vii)U.S. patent application Ser. No. 11/602,173, filed Nov. 20, 2006,“Systems And Methods Allowing For Reservoir Filling And Infusion MediumDelivery”; (viii) U.S. patent application Ser. No. 11/602,052, filedNov. 20, 2006, “Systems And Methods Allowing For Reservoir Filling AndInfusion Medium Delivery”; (ix) U.S. patent application Ser. No.11/602,428, filed Nov. 20, 2006, “Systems And Methods Allowing ForReservoir Filling And Infusion Medium Delivery”; (x) U.S. patentapplication Ser. No. 11/602,113, filed Nov. 20, 2006, “Systems AndMethods Allowing For Reservoir Filling And Infusion Medium Delivery”;(xi) U.S. patent application Ser. No. 11/604,171, filed Nov. 22, 2006,“Infusion Medium Delivery Device And Method With Drive Device ForDriving Plunger In Reservoir”; (xii) U.S. patent application Ser. No.11/604,172, filed Nov. 22, 2006, “Infusion Medium Delivery Device AndMethod With Drive Device For Driving Plunger In Reservoir”; (xiii) U.S.patent application Ser. No. 11/606,703, filed Nov. 30, 2006, “InfusionPumps And Methods And Delivery Devices And Methods With Same”; (xiv)U.S. patent application Ser. No. 11/606,836, filed Nov. 30, 2006,“Infusion Pumps And Methods And Delivery Devices And Methods With Same”;U.S. patent application Ser. No. 11/636,384, filed Dec. 8, 2006,“Infusion Medium Delivery Device And Method With Compressible Or CurvedReservoir Or Conduit”; (xv) U.S. patent application Ser. No. 11/645,993,filed Dec. 26, 2006, “Infusion Medium Delivery Device And Method WithCompressible Or Curved Reservoir Or Conduit”; U.S. patent applicationSer. No. 11/645,972, filed Dec. 26, 2006, “Infusion Medium DeliverySystem, Device And Method With Needle Inserter And Needle InserterDevice And Method”; (xvi) U.S. patent application Ser. No. 11/646,052,filed Dec. 26, 2006, “Infusion Medium Delivery System, Device And MethodWith Needle Inserter And Needle Inserter Device And Method”; (xvii) U.S.patent application Ser. No. 11/645,435, filed Dec. 26, 2006, “InfusionMedium Delivery System, Device And Method With Needle Inserter AndNeedle Inserter Device And Method”; (xviii) U.S. patent application Ser.No. 11/646,000, filed Dec. 26, 2006, “Infusion Medium Delivery System,Device And Method With Needle Inserter And Needle Inserter Device AndMethod”; (xix) U.S. patent application Ser. No. 11/759,725, filed Jun.7, 2007, “Infusion Medium Delivery Device And Method With Drive DeviceFor Driving Plunger In Reservoir”; (xx) U.S. patent application Ser. No.11/606,837, filed Nov. 30, 2006, “Method And Apparatus For Enhancing TheIntegrity Of An Implantable Sensor Device”; (xxi) U.S. patentapplication Ser. No. 11/702,713, filed Feb. 5, 2007, “Selective PottingFor Controlled Failure And Electronic Devices Employing The Same”;(xxii) U.S. patent application Ser. No. 11/843,601, filed Aug. 22, 2007,“System And Method For Sensor Recalibration”; (xxiii) U.S. patentapplication Ser. No. 11/868,898, filed Oct. 8, 2007, “MultilayerSubstrate”; (xxiv) U.S. patent application Ser. No. 11/964,649, filedDec. 26, 2007, “System And Methods Allowing For Reservoir Air BubbleManagement”; (xxv) U.S. patent application Ser. No. 12/111,751, filedApr. 29, 2008, “Systems And Methods For Reservoir Filling”; (xxvi) U.S.patent application Ser. No. 12/111,815, filed Apr. 29, 2008, “SystemsAnd Methods For Reservoir Air Bubble Management”; (xxvii) U.S. patentapplication Ser. No. 11/924,402, filed Oct. 25, 2007, “Sensor SubstrateAnd Method Of Fabricating Same”; (xxviii) U.S. patent application Ser.No. 11/929,428, filed Oct. 30, 2007, “Telemetry System And Method WithVariable Parameters”; (xxix) U.S. patent application Ser. No.11/965,578, filed Dec. 27, 2007, “Reservoir Pressure EqualizationSystems And Methods”; (xxx) U.S. patent application Ser. No. 12/107,580,filed Apr. 22, 2008, “Automative Filling Systems And Methods”; (xxxi)U.S. patent application Ser. No. 11/964,663, filed Dec. 26, 2007,“Medical Device With Full Options And Selective Enablement/Disablement”;(xxxii) U.S. patent application Ser. No. 10/180,732, filed Jun. 26,2002, “Communication Station And Software For Interfacing With AnInfusion Pump, Analyte Monitor, Analyte Meter, Or The Like”; (xxxiii)U.S. patent application Ser. No. 12/099,738, filed Apr. 8, 2008,“Systems And Methods Allowing For Reservoir Air Bubble Management”;(xxxiv) U.S. patent application Ser. No. 12/027,963, filed Feb. 7, 2008,“Adhesive Patch Systems And Methods”; (xxxv) U.S. patent applicationSer. No. 12/121,647, filed May 15, 2008, “Multi-Lumen Catheter”; (xxxvi)U.S. Patent Provisional Application Ser. No. 61/044,269, filed Apr. 11,2008, “Reservoir Plunger Head Systems And Methods”; (xxxvii) U.S. PatentApplication Ser. No. 61/044,292, filed Apr. 11, 2008, “Reservoir BarrierLayer Systems And Methods”; (xxxviii) U.S. Patent ProvisionalApplication Ser. No. 61/044,322, filed Apr. 11, 2008, “Reservoir SealRetainer Systems And Methods”; (xxxix) U.S. patent application Ser. No.12/179,502, filed Jul. 24, 2008, “Method For Formulating AndImmobilizing A Matrix Protein And A Matrix Protein For Use In A Sensor”;(xl) U.S. patent application Ser. No. 12/336,367, filed Dec. 16, 2008,“Needle Insertions Systems And Methods”; (xli) U.S. patent applicationSer. No. 12/166,210, filed Jul. 1, 2008, “Electronic Device ForControlled Failure”; (xlii) U.S. patent application Ser. No. 12/271,134,filed Nov. 14, 2008, “Multilayer Circuit Devices And ManufacturingMethods Using Electroplated Sacrificial Structures”; (xliii) U.S. patentapplication Ser. No. 12/171,971, filed Jul. 11, 2008, “Infusion MediumDelivery System, Device And Method With Needle Inserter And NeedleInserter Device And Method”; (xliv) U.S. patent application Ser. No.12/189,077, filed Aug. 8, 2008, “Packaging System”; (xlv) U.S. patentapplication Ser. No. 12/179,536, filed Jul. 24, 2008, “Real TimeSelf-Adjusting Calibration Algorithm”; (xlvii) U.S. patent applicationSer. No. 12/277,186, filed Nov. 24, 2008, “Infusion Medium DeliverySystem, Device And Method With Needle Inserter And Needle InserterDevice And Method”; (xlviii) U.S. patent application Ser. No.12/211,783, filed Sep. 16, 2008, “Implantable Sensor Method And System”;(xlix) U.S. patent application Ser. No. 12/247,945, filed Oct. 8, 2008,“Infusion Medium Delivery Device And Method With Drive Device ForDriving Plunger In Reservoir”; (l) U.S. patent application Ser. No.12/360,077, filed Jan. 26, 2009, “Reservoir Barrier Layer Systems AndMethods”; (li) U.S. patent application Ser. No. 12/345,362, filed Dec.29, 2008, “Reservoir Seal Retainer Systems And Methods”; (lii) U.S.patent application Ser. No. 12/353,181, filed Jan. 13, 2009, “SystemsAnd Methods Allowing For Reservoir Filling And Infusion MediumDelivery”; and (liii) U.S. patent application Ser. No. 12/360,813, filedJan. 27, 2009, “Multi-Position Infusion Set Device And Process.” Inother embodiments, the system 10, delivery device 12, sensing device 14,CCD 16, and computer 18 may have other suitable configurations.

The delivery device 12 may be configured to deliver fluidic media to thebody 5 of the user-patient 7. In various embodiments, fluidic media mayinclude a liquid, a fluid, a gel, or the like. In some embodiments,fluidic media may include a medicine or a drug for treating a disease ora medical condition. For example, fluidic media may include insulin fortreating diabetes, or may include a drug for treating pain, cancer, apulmonary disorder, HIV, or the like. In some embodiments, fluidic mediamay include a nutritional supplement, a dye, a tracing medium, a salinemedium, a hydration medium, or the like.

The sensing device 14 may include a sensor, a monitor, or the like, forproviding sensor data or monitor data. In various embodiments, thesensing device 14 may be configured to sense a condition of theuser-patient 7. For example, the sensing device 14 may includeelectronics and enzymes reactive to a biological condition, such as ablood glucose level, or the like, of the user-patient 7.

In various embodiments, the sensing device 14 may be secured to the body5 of the user-patient 7 or embedded in the body 5 of the user-patient 7at a location that is remote from the location at which the deliverydevice 12 is secured to the body 5 of the user-patient 7. In variousother embodiments, the sensing device 14 may be incorporated within thedelivery device 12. In other embodiments, the sensing device 14 may beseparate and apart from the delivery device, and may be, for example,part of the CCD 16. In such embodiments, the sensing device 14 may beconfigured to receive a biological sample, analyte, or the like, tomeasure a condition of the user-patient 7.

In further embodiments, the sensing device 14 and/or the delivery device12 may utilize a closed-loop system. Examples of sensing devices and/ordelivery devices utilizing closed-loop systems may be found at, but arenot limited to, the following references: (i) U.S. Pat. No. 6,088,608,entitled “Electrochemical Sensor And Integrity Tests Therefor”; (ii)U.S. Pat. No. 6,119,028, entitled “Implantable Enzyme-Based MonitoringSystems Having Improved Longevity Due To Improved Exterior Surfaces”;(iii) U.S. Pat. No. 6,589,229, entitled “Implantable Enzyme-BasedMonitoring Systems Adapted for Long Term Use”; (iv) U.S. Pat. No.6,740,072, entitled “System And Method For Providing Closed LoopInfusion Formulation Delivery”; (v) U.S. Pat. No. 6,827,702, entitled“Safety Limits For Closed-Loop Infusion Pump Control”; (vi) U.S. Pat.No. 7,323,142, entitled “Sensor Substrate And Method Of FabricatingSame”; (vii) U.S. patent application Ser. No. 09/360,342, filed Jul. 22,1999, entitled “Substrate Sensor”; and (viii) U.S. Provisional PatentApplication Ser. No. 60/318,060, filed Sep. 7, 2001, entitled “SensingApparatus and Process”, all of which are incorporated herein byreference in their entirety.

In such embodiments, the sensing device 14 may be configured to sense acondition of the user-patient 7, such as, but not limited to, bloodglucose level, or the like. The delivery device 12 may be configured todeliver fluidic media in response to the condition sensed by the sensingdevice 14. In turn, the sensing device 14 may continue to sense a newcondition of the user-patient, allowing the delivery device 12 todeliver fluidic media continuously in response to the new conditionsensed by the sensing device 14 indefinitely. In some embodiments, thesensing device 14 and/or the delivery device 12 may be configured toutilize the closed-loop system only for a portion of the day, forexample only when the user-patient is asleep or awake.

Each of the delivery device 12, the sensing device 14, the CCD 16, andthe computer 18 may include transmitter, receiver, or transceiverelectronics that allow for communication with other components of thesystem 10. The sensing device 14 may be configured to transmit sensordata or monitor data to the delivery device 12. The sensing device 14may also be configured to communicate with the CCD 16. The deliverydevice 12 may include electronics and software that are configured toanalyze sensor data and to deliver fluidic media to the body 5 of theuser-patient 7 based on the sensor data and/or preprogrammed deliveryroutines.

The CCD 16 and the computer 18 may include electronics and othercomponents configured to perform processing, delivery routine storage,and to control the delivery device 12. By including control functions inthe CCD 16 and/or the computer 18, the delivery device 12 may be madewith more simplified electronics. However, in some embodiments, thedelivery device 12 may include all control functions, and may operatewithout the CCD 16 and the computer 18. In various embodiments, the CCD16 may be a portable electronic device. In addition, in variousembodiments, the delivery device 12 and/or the sensing device 14 may beconfigured to transmit data to the CCD 16 and/or the computer 18 fordisplay or processing of the data by the CCD 16 and/or the computer 18.

In some embodiments, the sensing device 14 may be integrated into theCCD 16. Such embodiments may allow the user-patient to monitor acondition by providing, for example, a sample of his or her blood to thesensing device 14 to assess his or her condition. In some embodiments,the sensing device 14 and the CCD 16 may be for determining glucoselevels in the blood and/or body fluids of the user-patient without theuse of, or necessity of, a wire or cable connection between the deliverydevice 12 and the sensing device 14 and/or the CCD 16.

In some embodiments, the CCD 16 may be for providing information to theuser-patient that facilitates the user-patient's subsequent use of adrug delivery system. For example, the CCD 16 may provide information tothe user-patient to allow the user-patient to determine the rate or doseof medication to be administered into the body of the user-patient. Inother embodiments, the CCD 16 may provide information to the deliverydevice 12 to control the rate or dose of medication administered intothe body of the user-patient

Examples of the types of communications and/or control capabilities, aswell as device feature sets and/or program options may be found in thefollowing references: (i) U.S. patent application Ser. No. 10/445,477,filed May 27, 2003, entitled “External Infusion Device with RemoteProgramming, Bolus Estimator and/or Vibration Alarm Capabilities”; (ii)U.S. patent application Ser. No. 10/429,385, filed May 5, 2003, entitled“Handheld Personal Data Assistant (PDA) with a Medical Device and Methodof Using the Same”; and (iii) U.S. patent application Ser. No.09/813,660, filed Mar. 21, 2001, entitled “Control Tabs for InfusionDevices and Methods of Using the Same,” all of which are incorporatedherein by reference in their entirety.

FIG. 2 illustrates an example of the system 10 in accordance with anembodiment of the present invention. The system 10 in accordance withthe embodiment illustrated in FIG. 2 includes the delivery device 12 andthe sensing device 14. The delivery device 12 in accordance with anembodiment of the present invention includes a disposable housing 20, adurable housing 30, and a reservoir system 40. The delivery device 12may further include an infusion path 50.

Elements of the delivery device 12 that ordinarily contact the body of auser-patient or that ordinarily contact fluidic media during operationof the delivery device 12 may be considered as a disposable portion ofthe delivery device 12. For example, a disposable portion of thedelivery device 12 may include the disposable housing 20 and thereservoir system 40. The disposable portion of the delivery device 12may be recommended for disposal after a specified number of uses.

On the other hand, elements of the delivery device 12 that do notordinarily contact the body of the user-patient or fluidic media duringoperation of the delivery device 12 may be considered as a durableportion of the delivery device 12. For example, a durable portion of thedelivery device 12 may include the durable housing 30, electronics (notshown in FIG. 2), a drive device having a motor and drive linkage (notshown in FIG. 2), and the like. Elements of the durable housing portionof the delivery device 12 are typically not contaminated from contactwith the user-patient or fluidic media during normal operation of thedelivery device 12 and, thus, may be retained for re-use with replaceddisposable portions of the delivery device 12.

In various embodiments, the disposable housing 20 supports the reservoirsystem 40 and has a bottom surface (facing downward and into the page inFIG. 2) that is configured to secure to the body of a user-patient. Anadhesive may be employed at an interface between the bottom surface ofthe disposable housing 20 and the skin of a user-patient to adhere thedisposable housing 20 to the skin of the user-patient. In variousembodiments, the adhesive may be provided on the bottom surface of thedisposable housing 20, with a peelable cover layer covering the adhesivematerial. In this manner, the cover layer may be peeled off to exposethe adhesive material, and the adhesive side of the disposable housing20 may be placed against the user-patient, for example against the skinof the user-patient. Thus in some embodiments, the delivery device 12may be attached to the skin of the user-patient.

In other embodiments, the disposable housing 20 and/or the remainingportions of the delivery device 12 may be worn or otherwise attached onor underneath clothing of the user-patient. Similarly, the deliverydevice 12 may be supported by any suitable manner, such as, but notlimited to, on a belt, in a pocket, and the like. Representativeexamples of such delivery devices 12 may include, but is not limited to,the MiniMed Paradigm 522 Insulin Pump, MiniMed Paradigm 722 InsulinPump, MiniMed Paradigm 515 Insulin Pump, MiniMed Paradigm 715 InsulinPump, MiniMed Paradigm 512R Insulin Pump, MiniMed Paradigm 712R InsulinPump, MiniMed 508 Insulin Pump, MiniMed 508R Insulin Pump, and any otherderivatives thereof.

The reservoir system 40 is configured for containing or holding fluidicmedia, such as, but not limited to insulin. In various embodiments, thereservoir system 40 includes a hollow interior volume for receivingfluidic media, such as, but not limited to, a cylinder-shaped volume, atubular-shaped volume, or the like. In some embodiments, the reservoirsystem 40 may be provided as a cartridge or canister for containingfluidic media. In various embodiments, the reservoir system 40 is ableto be refilled with fluidic media. In further embodiments, the reservoirsystem 40 is pre-filled with fluidic media.

The reservoir system 40 may be supported by the disposable housing 20 inany suitable manner. For example, the disposable housing 20 may beprovided with projections or struts (not shown), or a trough feature(not shown), for holding the reservoir system 40. In some embodiments,the reservoir system 40 may be supported by the disposable housing 20 ina manner that allows the reservoir system 40 to be removed from thedisposable housing 20 and replaced with another reservoir.Alternatively, or in addition, the reservoir system 40 may be secured tothe disposable housing 20 by a suitable adhesive, a strap, or othercoupling structure.

In various embodiments, the reservoir system 40 includes a port 41 forallowing fluidic media to flow into and/or flow out of the interiorvolume of the reservoir system 40. In some embodiments, the infusionpath 50 includes a connector 56, a tube 54, and a needle apparatus 52.The connector 56 of the infusion path 50 may be connectable to the port41 of the reservoir system 40. In various embodiments, the disposablehousing 20 is configured with an opening near the port 41 of thereservoir system 40 for allowing the connector 56 of the infusion path50 to be selectively connected to and disconnected from the port 41 ofthe reservoir system 40.

In various embodiments, the port 41 of the reservoir system 40 iscovered with or supports a septum (not shown in FIG. 2), such as aself-sealing septum, or the like. The septum may be configured toprevent fluidic media from flowing out of the reservoir system 40through the port 41 when the septum is not pierced. In addition, invarious embodiments, the connector 56 of the infusion path 50 includes aneedle for piercing the septum covering the port 41 of the reservoirsystem 40 to allow fluidic media to flow out of the interior volume ofthe reservoir system 40.

Examples of needle/septum connectors can be found in U.S. patentapplication Ser. No. 10/328,393, filed Dec. 22, 2003, entitled“Reservoir Connector,” which is incorporated herein by reference in itsentirety. In other alternatives, non-septum connectors such as Luerlocks, or the like may be used. In various embodiments, the needleapparatus 52 of the infusion path 50 includes a needle that is able topuncture the skin of a user-patient. In addition, in variousembodiments, the tube 54 connects the connector 56 with the needleapparatus 52 and is hollow, such that the infusion path 50 is able toprovide a path to allow for the delivery of fluidic media from thereservoir system 40 to the body of a user-patient.

The durable housing 30 of the delivery device 12 in accordance withvarious embodiments of the present invention includes a housing shellconfigured to mate with and secure to the disposable housing 20. Thedurable housing 30 and the disposable housing 20 may be provided withcorrespondingly shaped grooves, notches, tabs, or other suitablefeatures, that allow the two parts to easily connect together, bymanually pressing the two housings together, by twist or threadedconnection, or other suitable manner of connecting the parts that iswell known in the mechanical arts.

In various embodiments, the durable housing 30 and the disposablehousing 20 may be connected to each other using a twist action. Thedurable housing 30 and the disposable housing 20 may be configured to beseparable from each other when a sufficient force is applied todisconnect the two housings from each other. For example, in someembodiments the disposable housing 20 and the durable housing 30 may besnapped together by friction fitting. In various embodiments, a suitableseal, such as an o-ring seal, may be placed along a peripheral edge ofthe durable housing 30 and/or the disposable housing 20, to provide aseal against water entering between the durable housing 30 and thedisposable housing 20.

The durable housing 30 of the delivery device 12 may support a drivedevice (not shown in FIG. 2), including a motor and a drive devicelinkage portion, for applying a force to fluidic media within thereservoir system 40 to force fluidic media out of the reservoir system40 and into an infusion path, such as the infusion path 50, for deliveryto a user-patient. For example, in some embodiments, an electricallydriven motor may be mounted within the durable housing 30 withappropriate linkage for operatively coupling the motor to a plunger arm(not shown in FIG. 2) connected to a plunger head (not shown in FIG. 2)that is within the reservoir system 40 and to drive the plunger head ina direction to force fluidic media out of the port 41 of the reservoirsystem 40 and to the user-patient.

Also, in some embodiments, the motor may be controllable to reversedirection to move the plunger arm and the plunger head to cause fluid tobe drawn into the reservoir system 40 from a patient. The motor may bearranged within the durable housing 30 and the reservoir system 40 maybe correspondingly arranged on the disposable housing 20, such that theoperable engagement of the motor with the plunger head, through theappropriate linkage, occurs automatically upon the user-patientconnecting the durable housing 30 with the disposable housing 20 of thedelivery device 12. Further examples of linkage and control structuresmay be found in U.S. patent application Ser. No. 09/813,660, filed Mar.21, 2001, entitled “Control Tabs for Infusion Devices and Methods ofUsing the Same”, which is incorporated herein by reference in itsentirety.

In various embodiments, the durable housing 30 and the disposablehousing 20 may be made of suitably rigid materials that maintain theirshape, yet provide sufficient flexibility and resilience to effectivelyconnect together and disconnect, as described above. The material of thedisposable housing 20 may be selected for suitable compatibility withskin. For example, the disposable housing 20 and the durable housing 30of the delivery device 12 may be made of any suitable plastic, metal,composite material, or the like. The disposable housing 20 may be madeof the same type of material or a different material relative to thedurable housing 30. In some embodiments, the disposable housing 20 andthe durable housing 30 may be manufactured by injection molding or othermolding processes, machining processes, or combinations thereof.

For example, the disposable housing 20 may be made of a relativelyflexible material, such as a flexible silicone, plastic, rubber,synthetic rubber, or the like. By forming the disposable housing 20 of amaterial capable of flexing with the skin of a user-patient, a greaterlevel of user-patient comfort may be achieved when the disposablehousing 20 is secured to the skin of the user-patient. In addition, aflexible disposable housing 20 may result in an increase in site optionson the body of the user-patient at which the disposable housing 20 maybe secured.

In the embodiment illustrated in FIG. 2, the delivery device 12 isconnected to the sensing device 14 through a connection element 17 ofthe sensing device 14. The sensing device 14 may include a sensor 15that includes any suitable biological or environmental sensing device,depending upon a nature of a treatment to be administered by thedelivery device 12. For example, in the context of delivering insulin toa diabetes patient, the sensor 15 may include a blood glucose sensor, orthe like.

In some embodiments, the sensor 15 may include a continuous glucosesensor. The continuous glucose sensor may be implantable within the bodyof the user-patient. In other embodiments, the continuous glucose sensormay be located externally, for example on the skin of the user-patient,or attached to clothing of the user-patient. In such embodiments, fluidmay be drawn continually from the user-patient and sensed by thecontinuous glucose sensor. In various embodiments, the continuousglucose sensor may be configured to sense and/or communicate with theCCD 16 continuously. In other embodiments, the continuous glucose sensormay be configured to sense and/or communicate with the CCD 16intermittently, for example sense glucose levels and transmitinformation every few minutes. In various embodiments, the continuousglucose sensor may utilize glucose oxidase.

The sensor 15 may be an external sensor that secures to the skin of auser-patient or, in other embodiments, may be an implantable sensor thatis located in an implant site within the body of the user-patient. Infurther alternatives, the sensor may be included with as a part or alongside the infusion cannula and/or needle, such as for example as shown inU.S. patent application Ser. No. 11/149,119, filed Jun. 8, 2005,entitled “Dual Insertion Set”, which is incorporated herein by referencein its entirety. In the illustrated example of FIG. 2, the sensor 15 isan external sensor having a disposable needle pad that includes a needlefor piercing the skin of the user-patient and enzymes and/or electronicsreactive to a biological condition, such as blood glucose level or thelike, of the user-patient. In this manner, the delivery device 12 may beprovided with sensor data from the sensor 15 secured to the user-patientat a site remote from the location at which the delivery device 12 issecured to the user-patient.

While the embodiment shown in FIG. 2 includes a sensor 15 connected bythe connection element 17 for providing sensor data to sensorelectronics (not shown in FIG. 2) located within the durable housing 30of the delivery device 12, other embodiments may employ a sensor 15located within the delivery device 12. Yet other embodiments may employa sensor 15 having a transmitter for communicating sensor data by awireless communication link with receiver electronics (not shown in FIG.2) located within the durable housing 30 of the delivery device 12. Invarious embodiments, a wireless connection between the sensor 15 and thereceiver electronics within the durable housing 30 of the deliverydevice 12 may include a radio frequency (RF) connection, an opticalconnection, or another suitable wireless communication link. Furtherembodiments need not employ the sensing device 14 and, instead, mayprovide fluidic media delivery functions without the use of sensor data.

As described above, by separating disposable elements of the deliverydevice 12 from durable elements, the disposable elements may be arrangedon the disposable housing 20, while durable elements may be arrangedwithin a separable durable housing 30. In this regard, after aprescribed number of uses of the delivery device 12, the disposablehousing 20 may be separated from the durable housing 30, so that thedisposable housing 20 may be disposed of in a proper manner. The durablehousing 30 may then be mated with a new (un-used) disposable housing 20for further delivery operation with a user-patient.

FIG. 3 illustrates an example of the delivery device 12 in accordancewith another embodiment of the present invention. The delivery device 12of the embodiment of FIG. 3 is similar to the delivery device 12 of theembodiment of FIG. 2. While the delivery device 12 in the embodimentillustrated in FIG. 2 provides for the durable housing 30 to cover thereservoir system 40, the delivery device 12 in the embodiment of FIG. 3provides for the durable housing 30 to secure to the disposable housing20 without covering the reservoir system 40. The delivery device 12 ofthe embodiment illustrated in FIG. 3 includes the disposable housing 20,and the disposable housing 20 in accordance with the embodimentillustrated in FIG. 3 includes a base 21 and a reservoir retainingportion 24. In one embodiment, the base 21 and reservoir retainingportion 24 may be formed as a single, unitary structure.

The base 21 of the disposable housing 20 is configured to be secured tothe body of a user-patient. The reservoir retaining portion 24 of thedisposable housing 20 is configured to house the reservoir system 40.The reservoir retaining portion 24 of the disposable housing 20 may beconfigured to have an opening to allow for the port 41 of the reservoirsystem 40 to be accessed from outside of the reservoir retaining portion24 while the reservoir system 40 is housed in the reservoir retainingportion 24. The durable housing 30 may be configured to be attachable toand detachable from the base 21 of the disposable housing 20. Thedelivery device 12 in the embodiment illustrated in FIG. 3 includes aplunger arm 60 that is connected to or that is connectable to a plungerhead (not shown in FIG. 3) within the reservoir system 40.

FIG. 4 illustrates another view of the delivery device 12 of theembodiment of FIG. 3. The delivery device 12 of the embodimentillustrated in FIG. 4 includes the disposable housing 20, the durablehousing 30, and the infusion path 50. The disposable housing 20 in theembodiment of FIG. 4 includes the base 21, the reservoir retainingportion 24, and a peelable cover layer 25. The peelable cover layer 25may cover an adhesive material on the bottom surface 22 of the base 21.The peelable cover layer 25 may be configured to be peelable by auser-patient to expose the adhesive material on the bottom surface 22 ofthe base 21. In some embodiments, there may be multiple adhesive layerson the bottom surface 22 of the base 21 that are separated by peelablelayers.

The infusion path 50 in accordance with the embodiment of the presentinvention illustrated in FIG. 4 includes the needle 58 rather than theconnector 56, the tube 54, and the needle apparatus 52 as shown in theembodiment of FIG. 2. The base 21 of the disposable housing 20 may beprovided with an opening or pierceable wall in alignment with a tip ofthe needle 58, to allow the needle 58 to pass through the base 21 andinto the skin of a user-patient under the base 21, when extended. Inthis manner, the needle 58 may be used to pierce the skin of theuser-patient and deliver fluidic media to the user-patient.

Alternatively, the needle 58 may be extended through a hollow cannula(not shown in FIG. 4), such that upon piercing the skin of theuser-patient with the needle 58, an end of the hollow cannula is guidedthrough the skin of the user-patient by the needle 58. Thereafter, theneedle 58 may be removed, leaving the hollow cannula in place, with oneend of the cannula located within the body of the user-patient and theother end of the cannula in fluid flow connection with fluidic mediawithin the reservoir system 40, to convey pumped infusion media from thereservoir system 40 to the body of the user-patient.

FIG. 5A illustrates a durable portion 8 of the delivery device 12 (referto FIG. 3) in accordance with an embodiment of the present invention.FIG. 5B illustrates a section view of the durable portion 8 inaccordance with an embodiment of the present invention. FIG. 5Cillustrates another section view of the durable portion 8 in accordancewith an embodiment of the present invention. With reference to FIGS. 5A,5B, and 5C, in various embodiments, the durable portion 8 includes thedurable housing 30, and a drive device 80. The drive device 80 includesa motor 84 and a drive device linkage portion 82.

In various embodiments, the durable housing 30 may include an interiorvolume for housing the motor 84, the drive device linkage portion 82,other electronic circuitry, and a power source (not shown in FIGS. 5A,5B, and 5C). In addition, in various embodiments, the durable housing 30is configured with an opening 32 for receiving a plunger arm 60 (referto FIG. 3). In addition, in various embodiments, the durable housing 30may include one or more connection members 34, such as tabs, insertionholes, or the like, for connecting with the base 21 of the disposablehousing 20 (refer to FIG. 3).

FIG. 6A illustrates a disposable portion 9 of the delivery device 12(refer to FIG. 3) in accordance with an embodiment of the presentinvention. FIG. 6B illustrates a section view of the disposable portion9 in accordance with an embodiment of the present invention. FIG. 6Cillustrates another section view of the disposable portion 9 inaccordance with an embodiment of the present invention. With referenceto FIGS. 6A, 6B, and 6C, in various embodiments, the disposable portion9 includes the disposable housing 20, the reservoir system 40, theplunger arm 60, and a plunger head 70. In some embodiments, thedisposable housing 20 includes the base 21 and the reservoir retainingportion 24. In various embodiments, the base 21 includes a top surface23 having one or more connection members 26, such as tabs, grooves, orthe like, for allowing connections with the one or more connectionmembers 34 of embodiments of the durable housing 30 (refer to FIG. 5B).

In various embodiments, the reservoir system 40 is housed within thereservoir retaining portion 24 of the disposable housing 20, and thereservoir system 40 is configured to hold fluidic media. In addition, invarious embodiments, the plunger head 70 is disposed at least partiallywithin the reservoir system 40 and is moveable within the reservoirsystem 40 to allow fluidic media to fill into the reservoir system 40and to force fluidic media out of the reservoir system 40. In someembodiments, the plunger arm 60 is connected to or is connectable to theplunger head 70.

Also, in some embodiments, a portion of the plunger arm 60 extends tooutside of the reservoir retaining portion 24 of the disposable housing20. In various embodiments, the plunger arm 60 has a mating portion formating with the drive device linkage portion 82 of the drive device 80(refer to FIG. 5C). With reference to FIGS. 5C and 6C, in someembodiments, the durable housing 30 may be snap fitted onto thedisposable housing 20, whereupon the drive device linkage portion 82automatically engages the mating portion of the plunger arm 60.

When the durable housing 30 and the disposable housing 20 are fittedtogether with the drive device linkage portion 82 engaging or matingwith the plunger arm 60, the motor 84 may be controlled to drive thedrive device linkage portion 82 and, thus, move the plunger arm 60 tocause the plunger head 70 to move within the reservoir system 40. Whenthe interior volume of the reservoir system 40 is filled with fluidicmedia and an infusion path is provided from the reservoir system 40 tothe body of a user-patient, the plunger head 70 may be moved within thereservoir system 40 to force fluidic media from the reservoir system 40and into the infusion path, so as to deliver fluidic media to the bodyof the user-patient.

In various embodiments, once the reservoir system 40 has beensufficiently emptied or otherwise requires replacement, a user-patientmay simply remove the durable housing 30 from the disposable housing 20,and replace the disposable portion 9, including the reservoir system 40,with a new disposable portion having a new reservoir. The durablehousing 30 may be connected to the new disposable housing of the newdisposable portion, and the delivery device including the new disposableportion may be secured to the skin of a user-patient, or otherwiseattached to the user-patient.

In various other embodiments, rather than replacing the entiredisposable portion 9 every time the reservoir system 40 is emptied, thereservoir system 40 may be refilled with fluidic media. In someembodiments, the reservoir system 40 may be refilled while remainingwithin the reservoir retaining portion 24 (refer to FIG. 6B) of thedisposable housing 20. In addition, in various embodiments, thereservoir system 40 may be replaced with a new reservoir (not shown),while the disposable housing 20 may be re-used with the new reservoir.In such embodiments, the new reservoir may be inserted into thedisposable portion 9.

With reference to FIGS. 3, 5A, 6B, and 6C, in various embodiments, thedelivery device 12 includes reservoir status circuitry (not shown), andthe reservoir system 40 includes reservoir circuitry (not shown). Invarious embodiments, the reservoir circuitry stores information such as,but not limited to, at least one of (i) an identification stringidentifying the reservoir system 40; (ii) a manufacturer of thereservoir system 40; (iii) contents of the reservoir system 40; and (iv)an amount of contents in the reservoir system 40. In some embodiments,the delivery device 12 includes the reservoir status circuitry (notshown), and the reservoir status circuitry is configured to read datafrom the reservoir circuitry when the reservoir system 40 is insertedinto the disposable portion 9.

In various embodiments, the reservoir status circuitry is furtherconfigured to store data to the reservoir circuitry after at least someof the contents of the reservoir system 40 have been transferred out ofthe reservoir system 40, so as to update information in the reservoircircuitry related to an amount of contents still remaining in thereservoir system 40. In some embodiments, the reservoir status circuitryis configured to store data to the reservoir circuitry, to updateinformation in the reservoir circuitry related to an amount of contentsremaining in the reservoir system 40, when the reservoir system 40 isinserted into the disposable portion 9. In some embodiments, thedelivery device 12 includes the reservoir status circuitry (not shown)and the reservoir system 40 includes the reservoir circuitry (notshown), and the reservoir status circuitry selectively inhibits use ofthe delivery device 12 or selectively provides a warning signal based oninformation read by the reservoir status circuitry from the reservoircircuitry.

FIGS. 7-8C illustrate a system 100 for transferring fluidic media inaccordance with an embodiment of the present invention. The system 100may include features similar to, employed as an embodiment of, and/orused with the medical device systems discussed throughout the disclosure(e.g., delivery device 12 in FIGS. 1-6C). Although the system 100 mayinclude features similar or used with the embodiments of FIGS. 1-6C, itshould be understood that the system 100 may also include some or all ofthe same features and operate in a manner similar to that shown anddescribed in the embodiments of FIGS. 9-17. In addition, some or all ofthe features shown in FIGS. 1-6C and 9-17 may be combined in variousways and included in the embodiments shown in FIGS. 7-8C. Likewise, itshould be understood that any of the features of the embodiments ofFIGS. 7-8C may be combined or otherwise incorporated into any of theother embodiments of FIGS. 7-8C as well as any other embodiment hereindiscussed.

The system 100 may include, but is not limited to, a vial 140, atransfer guard 160, and a reservoir 180. The vial 140 may include aseptum 144 located at a port 142 of the vial 140. The vial 140 may havean interior volume 145 for containing fluidic media. The reservoir 180may have an interior volume 185 for containing fluidic media. Thereservoir 180 may include a septum 184 located at a port 182 of thereservoir 180.

The plunger head 190 may be located within the reservoir 180 and may bemoveable within the reservoir 180 to expand or contract the interiorvolume 185 of the reservoir 180. The plunger head 190 may be attached toor integrated with the plunger arm 110. The handle 130 may beoperatively to the plunger arm 110.

The plunger head 190 may include at least one seal member 199, such asan o-ring, or the like, in contact with the reservoir 180. The interiorvolume 185 of the reservoir body 180 may be on one side of the sealmember 199. The reservoir 180 may have a chamber 187 located on anopposite side of the seal member 199 from the interior volume 185 of thereservoir 180. The seal member 199 may be for facilitating movementwithin the reservoir 180 and/or to substantially prevent fluidic mediafrom flowing from the interior volume 185 to the chamber 187 of thereservoir 180.

The transfer guard 160 may include a needle 152 for providing a fluidpath from the interior volume 145 of the vial 140 to the interior volume185 of the reservoir 180. The transfer guard 160 may be configured suchthat when the vial 140 is attached or otherwise mated to the transferguard 160, the needle 152 pierces the septum 144 of the vial 140. Thetransfer guard 160 may be further configured such that when thereservoir 180 is attached or otherwise mated to the transfer guard 160,the needle 152 pierces the septum 184 of the reservoir 180. Thus, thetransfer guard 160 may allow for establishing a fluid path from the vial140 to the reservoir 180 through the needle 152.

In some embodiments, the transfer guard 160 may include a second needle156. The second needle 156 may be able to pierce the septum 144 of thevial 140 when the vial 140 is connected to the transfer guard 160. Anend of the second needle 156 may be located within a headspace 147 ofthe vial 140 above fluidic media within the interior volume 145 of thevial 140 in a case where the transfer guard 160 is connected to the vial140. In other embodiments, the end of the second needle 156 may be incontact with fluidic media within the interior volume 145 of the vial140 in a case where the transfer guard 160 is connected to the vial 140.

Another end of the second needle 156 may be connected to a check valve154, such as a one-way valve, or the like. The check valve 154 may allowair to enter the interior volume 145 of the vial 140 through the secondneedle 156. In some embodiments, the check valve 154 may substantiallyprevent liquid from coming out of the vial 140 through the second needle156 and/or the check valve 154. In various embodiments, the secondneedle 156 may allow for venting the headspace 147 or the interiorvolume 145 of the vial 140 to atmosphere to facilitate the transfer offluidic media from the vial 140 to the reservoir 180.

The transfer guard 160 may have a body 165, a first end 162, and asecond end 170. The first end 162 may be for supporting or otherwisereceiving the vial 140 to attach or otherwise mate with the vial 140 tothe transfer guard 160. For example, a portion of the vial 140 (e.g.,portion corresponding to the port 142 of the vial 140) may be placed inthe first end 162 of the transfer guard 160. As described above, theseptum 144 of the vial 140 may be pierced by the needle 152 of thetransfer guard 160 when the vial 140 is inserted into the first end 162of the transfer guard 160.

In some embodiments, the first end 162 may be adapted to secure the vial140 to the transfer guard 160 in any suitable manner known in the art,such as (but not limited to) friction fitting, snap-fitting, or thelike. For example, the first end 162 of the transfer guard 160 mayinclude at least one tab 163, annular rib, or the like for securing thevial 140 within the first end 162 of the transfer guard 160 once thevial 140 is inserted in the first end 162 of the transfer guard 160.

The second end 170 may be located opposite the first end 162. The secondend 170 may be for supporting or otherwise receiving the reservoir 180to attach or otherwise mate with the reservoir 180 to the transfer guard160. For example, a portion of the reservoir 180 (e.g., portioncorresponding to the port 182 of the reservoir 180) may be placed in thesecond end 170 of the transfer guard 160. The septum 184 of thereservoir 180 may be pierced by the needle 152 of the transfer guard 160when the reservoir 180 is inserted into the second end 170 of thetransfer guard 160.

In some embodiments, the second end 170 may be adapted to secure thereservoir 180 to the transfer guard 160 in any suitable manner known inthe art, such as (but not limited to) friction fitting, snap-fitting, orthe like. For example, as shown in FIGS. 7 and 8A-8C, the second end 170of the transfer guard 160 may include one or more depressions orapertures 171 located within the second end 170 of the transfer guard160. The port 182 portion of the reservoir 180 may include one or moretabs 186 for inserting into the one or more apertures 171 located in thesecond end 170 of the transfer guard 160. The port 182 portion of thereservoir 180 may further include at least one second tab 188 attachedto each of the one or more tabs 186.

In some embodiments, the reservoir 180 and port 182 portion may beconfigured, for example, to be rotatable, at least partially, about thesecond end 170 of the transfer guard 160 to secure the reservoir 180 tothe transfer guard 160. The second end 170 of the transfer guard 160 mayfurther include one or more depressions 172 for receiving the at leastone second tab 188 when the reservoir 180 and port 182 portion arerotated to secure the reservoir 180 to the transfer guard 160. As aresult, the port 182 portion of the reservoir 180 may be inserted intothe second end 170 of the transfer guard 160 so that the one or moretabs 186 fit into the apertures 171 and then rotated slightly until theat least one second tab 188 fits into place within the one or moredepressions 172 to lock the reservoir 180 into the second end 170 of thetransfer guard 160.

In some embodiments, the first end 162 and the vial 140 may beconfigured in the same manner as described above so that the one or moretabs 186 fit into the one or more apertures 171 and adapted to berotatable slightly until the at least one second tab 188 fits into placewithin the one or more depressions 172. In some embodiments, the secondend 170 of the transfer guard 160 may be configured to include at leastone tab 163 for securing at least a portion of the reservoir 180 withinthe second end 170 of the transfer guard 160 similar to that describedabove with respect to the first end 162 of the transfer guard 160.

FIGS. 9-17 illustrates a system 200 for transferring fluidic media inaccordance with an embodiment of the present invention. The system 200may include features similar to, employed as an embodiment of, and/orused with the medical device systems discussed throughout the disclosure(e.g., delivery device 12 in FIGS. 1-6C). In addition, the system 200may include features similar to the systems discussed throughout thedisclosure or employed as an embodiments of the systems (e.g., system100 in FIGS. 7-8C) discussed throughout the disclosure. In addition,some or all of the features shown in FIGS. 1-8C may be combined invarious ways and included in the embodiments shown in FIG. 9-17.Likewise, it should be understood that any of the features of theembodiments of FIGS. 9-17 may be combined or otherwise incorporated intoany of the other embodiments of FIGS. 9-17 as well as any otherembodiment herein discussed.

In particular embodiments, the system 200 may be similar to the system100 described with respect to FIGS. 7-8C. As shown, for example in FIGS.9 and 10, the system 200 may include, but is not limited to, a vial 240,a transfer guard 260, a reservoir 280, a plunger head 290, a plunger arm210, a plunger arm casing 230, and a handle 220.

FIGS. 11-14B illustrate a reservoir 280, which may include featuressimilar to or employed as an embodiment of the reservoir 180 (e.g.,FIGS. 7 and 8C), that may be employed in the system 200 according tovarious embodiments of the present invention. As previously described,the reservoir 280 may have an interior volume 285 for containing fluidicmedia. The reservoir 280 may include a septum 284 located at a port 282of the reservoir 280. In various embodiments, the reservoir 280 may bemade of various suitable materials, including, but not limited to,glass, plastic, TOPAS® polymer (or any other cyclic olefin copolymer (orpolymer)), or the like. The reservoir 280 may be of any suitable shapeand/or size and may be adapted to hold any volume of fluidic mediadepending on needs of user-patients.

The port 282 may be for expelling fluidic media contained in theinterior volume 285 of the reservoir 280, for example, when thereservoir 280 is used with a delivery device (not shown) for deliveringfluidic media to a user-patient. In various embodiments, the port 282 ofthe reservoir 280 may be for allowing fluidic media to flow into theinterior volume 285 of the reservoir 280 (i.e., to fill the interiorvolume 285 of the reservoir 280), for example, from the vial 240 via theneedle 252 of the transfer guard 260. Thus, in some embodiments, theport 282 may allow for filling the reservoir 280, for example, whenconnected to the transfer guard 260 connected to the vial 240, and forexpelling fluidic media, for example, when connected to a deliverydevice.

In some embodiments, the port 282 may be near an edge of the reservoir280 to facilitate a purging of bubbles in the interior volume 285 of thereservoir 280. For example, the user-patient could tilt the reservoir280 (or the entire system 200) slightly to allow bubbles to escapethrough the port 282.

In some embodiments, an end 289 of the reservoir 280 may be open toallow the plunger head 290 and/or at least a portion of the plunger arm210 to be insertable into the reservoir 280. For example, in a casewhere the port 282 is located on a first end of the reservoir 280, asecond end opposite the first end may be the end 289 of the reservoir280.

The plunger head 290 or a portion thereof may be made of Bromobutylrubber, silicone rubber, or any other suitable material and/or anyderivative thereof. The plunger head 290 may be locatable within thereservoir 280 and may be moveable in an axial direction of the reservoir280 to expand or contract the interior volume 285 of the reservoir 280.The plunger head 290 may be advanced within the reservoir 280 to expelfluidic media contained in the interior volume 285 of the reservoir 280out the port 282 of the reservoir 280, for example, when the reservoir280 is used with the delivery device for delivering fluidic media to theuser-patient. In various embodiments, the plunger head 290 may beadapted to be moveable within the reservoir 280 to draw fluidic mediainto the reservoir 280 from the vial 240, for example, in a case wherethe reservoir 280 is connected to the transfer guard 260 and the vial240 is connected to the transfer guard 260.

The plunger head 290 may have a front portion 297 and a rear portion298. The front portion 297 of the plunger head 290 may be in contactwith fluidic media contained in the interior volume 285 of the reservoir280. In some embodiments, the front portion 297 of the plunger head 290may comprise a material compatible with fluidic media contained or to becontained in the interior volume 285 of the reservoir 280.

The rear portion 298 of the plunger head 290 may be connected orconnectable to an end of the plunger arm 210 in any suitable manner. Forexample, the rear portion 298 of the plunger head 290 may include atleast one aperture 291 or the like for receiving at least one tab 211 orthe like of the plunger arm 210. The at least one tab 211 may besnap-fit into the at least one aperture 291 to connect the plunger arm210 to the rear portion 298 of the plunger head 290. In someembodiments, the plunger head 290 may contain at least one tab 292 orthe like and the plunger arm 210 may include at least one aperture 212or the like for receiving the at least one tab 292. In various otherembodiments, the plunger arm 210 may be connected to the plunger head290 and/or the rear portion 298 of the plunger head 290 in any suitablemanner, such as, but not limited to, an adhesive, friction fitting,laser welding, magnetic coupling, or the like.

The plunger arm 210 may be moveable in an axial direction within theplunger arm casing 230 and the reservoir 280. In some embodiments, theplunger arm 210 and the rear portion 298 of the plunger head 290 may beintegral to one another. In such embodiments, the plunger arm 210 andthe integrated rear portion 298 may be integral with the plunger head290 or be connectable to the plunger head 290. In other embodiments, theplunger arm 210 and the rear portion 298 of the plunger head 290 may beseparate components adapted to be connected together as previouslydescribed.

The plunger arm 210 may include an engagement side 218 for operativelyengaging a drive member (not shown), drive linkage, or the like whenconnected to the delivery device. For example, the engagement side 218of the plunger arm 210 and the drive member may be complementing gears,complementing threaded or toothed members, or the like, that mayoperatively engage each other. The drive member may be a drive screw,drive rack, or the like.

The drive member may be operatively connected to a motor to move orotherwise actuate the drive member to actuate or otherwise cause theplunger arm 210 to move within the plunger arm casing 230 and/or thereservoir 280. Accordingly, the plunger arm 210 may move within thereservoir 280 to expand or contact the interior volume 285 of thereservoir 280 to fill the reservoir 280 with fluidic media or expelfluidic media from the reservoir 280. In some embodiments, the drivemotor may be operatively engaged or directly engaged with the engagementside 218 of the plunger arm 210 to actuate or otherwise cause theplunger arm 210 to move within the plunger arm casing 230 and/or thereservoir 280.

The plunger arm casing 230 may be for supporting the plunger arm 210 asthe plunger arm 210 is moved along the plunger arm casing 230 and/or thereservoir 280, for example, from actuation by the drive member or thehandle 220 (e.g., FIGS. 16A-17). At least one side of the plunger arm210 may be in contact with one or more interior sides of the plunger armcasing 230. In some embodiments, the plunger arm casing 230 may be foraligning or otherwise guiding the plunger arm 210, for example, into thereservoir 280 as the plunger arm 210 moves along the reservoir 280, forexample, from actuation by the drive member or the handle 270 (discussedlater). The casing 230 may be made of a material of suitable strengthand durability such as, but not limited to, plastic, metal, glass (e.g.,tempered glass), composite material, and/or the like. In someembodiments, the casing 230 may be made of the same material as thereservoir 280.

In various embodiments, the plunger arm casing 230 may be sized andconfigured to substantially or completely envelop the plunger arm 210,for example, when the plunger head 290 is drawn substantially near theend 289 of the reservoir 280 (e.g., in a case where the reservoir 280has been filled or substantially filled with fluidic media). Thus insome embodiments, the plunger arm 210 or a portion thereof may belocated within the reservoir 280 and/or the plunger arm casing 230during use of the system 200 for transferring fluidic media from thevial 240 to the reservoir 280 or during operation of the deliverydevice.

In some embodiments, the plunger arm casing 230 may have an opening 236for allowing a portion of the engagement side 218 of the plunger arm 210to operatively engage the drive member or drive motor. In suchembodiments, the plunger arm 210 may be surrounded by the plunger armcasing 230 and/or the reservoir 280 except for the portion of theengagement side 218 of the plunger arm 210 exposed by the opening 236,which may be free from (i.e., not surrounded by) the plunger arm casing230 and/or the reservoir 280. This may allow the drive member tooperatively engage the engagement side 218 of the plunger arm 210 whilethe plunger arm 210 or a portion thereof remains in the plunger armcasing 230 and/or the reservoir 280.

The system 200 may include a reservoir cover 234 that may be sized andconfigured to cover the end 289 of the reservoir 280. The reservoircover 234 may cover the end 289 of the reservoir 280 or be configured tofit within or to the end 289 of the reservoir 280 to seal or close theend 289 of the reservoir 280. The reservoir cover 234 may be integralwith or separate from the plunger arm casing 230. The reservoir cover234 may have an opening 233 (refer to FIG. 17) to allow the plunger arm210 to move into or out of the reservoir 280. The reservoir cover 234may be made of a material of suitable strength and durability such as,but not limited to, plastic, metal, glass (e.g., tempered glass),composite material, and/or the like. In some embodiments, the reservoircover 234 may be made of the same material as the plunger arm casing 230and/or the reservoir 280.

In some embodiments, the reservoir cover 234 and/or the plunger armcasing 230 may be configured for minimizing an expansion of thereservoir 280 in one or more dimensions. In such embodiments, by fittingthe reservoir cover 234 to the end 289 of the reservoir 280, thereservoir cover 234 may help retain a shape of the reservoir 280, forexample, as the interior volume 285 of the reservoir body 280 fills withfluidic media.

In some embodiments, the reservoir system 200 may include at least onesupport flange 217 positioned on the plunger arm 210 and the rearportion 298 of the plunger head 290. The support flange 217 may provideadditional structural strength to the plunger arm 210 and/or the plungerhead 290. For example, the support flange 217 may have a triangularconfiguration and be positioned with one side of the support flange 217connected to a surface of the plunger arm 210 and a second side of thesupport flange 217 connected to the rear portion 298 of the plunger head290.

In addition to or alternative to, a second support flange (not shown)may be positioned with one side of the second support flange connectedto a different surface of the plunger arm 210 and a second side of thesecond support flange connected to the rear portion 298 of the plungerhead 290. In various embodiments, support flanges may located along anysuitable location for providing support to the plunger arm 210 and/orthe plunger head 290 or any other component. One or both of the supportflanges may be made of a material of suitable strength and durabilitysuch as, but not limited to, plastic, metal, glass (e.g., temperedglass), composite material, and/or the like. In some embodiments, theone or both of the support flanges may be made of the same material asthe plunger arm casing 230, the reservoir cover 234, and/or thereservoir 280.

In some embodiments, the plunger arm casing 230 may include a groove 238or the like for allowing a portion of the handle 220 (e.g., FIGS.16A-17) to operatively engage the plunger arm 210. Thus, the handle 220may be operatively engaged to the plunger arm 210 through the groove 238to transfer force to actuate or otherwise move the plunger arm 210 alongthe plunger arm casing 230 and/or the reservoir 280.

With reference to FIGS. 9, 10, 12, 13, and 17, in various embodiments,the second end 270 may be connected to or integrated with the transferguard 260. The second end 270 may comprise a body 273. The body 273 mayhave a hollow interior 275 for removably receiving at least a portion ofthe reservoir 280. In further embodiments, the body 273 may be adaptedsuch that the reservoir 280 may be placed entirely in the hollowinterior 275 of the body 273. In embodiments where the port 282 islocated near an edge of the reservoir 280, the second end 270 may be offcenter from the transfer guard 260. The body 273 may be made of amaterial of suitable strength and durability such as, but not limitedto, plastic, metal, glass (e.g., tempered glass), composite material,and/or the like. In some embodiments, the body 273 may be made of thesame material as the transfer guard 260 or a portion thereof.

In some embodiments, the body 273 may include one or more fill lines 278or other indicators for providing information located, for example, on afront side 273 a of the body 273. In other embodiments, the one or morefill lines 278 may be arranged in any suitable manner or along anysuitable portion of the body 273. For instance, the one or more filllines 278 may correspond to amount(s) of fluidic media contained in thereservoir 280. Thus, for example, the user-patient can fill thereservoir 280 accurately with a specific amount (e.g., 0.5 ml, 1 ml,etc.) of fluidic media from the vial 240 by comparing an amount offluidic media in the interior volume 285 of the reservoir 280 with theone or more fill lines 278.

In some embodiments, an indicator 279 may be provided corresponding to alocation of the port 282 of the reservoir 280 in a case where thereservoir is mated with the second end 270. In such embodiments, theuser-patient can direct bubbles in the interior volume 285 of thereservoir 280 toward the indicator, for example by titling the reservoir280 or the system 200, to purge the bubbles.

In further embodiments, the body 273 may be adapted to allow auser-patient to view at least some contents in the reservoir 280. Forexample, portions of the body 273 may have an opening to expose at leasta portion of the reservoir 280 within the hollow interior 275 of thebody 273. In such embodiments, the user-patient may be able to hold thereservoir though the opening to further support the reservoir 280 duringuse of the system 200. As another example, the body 273 or portionsthereof may be at least partially transparent to visually expose atleast a portion of the reservoir 280 within the hollow interior 275 ofthe body 273.

In some embodiments, the body 273 may be configured to secure thereservoir 280 or a portion thereof in the hollow interior 275 once thereservoir 280 is placed in the hollow interior 275. For example, thebody 273 may have one or more tabs 277 or the like within the hollowinterior 275 for securing or otherwise preventing accidental removal ofthe reservoir 280 from the hollow interior 275.

In some embodiments, the body 273 may be adapted to be flexible. Thismay allow, for example, the user-patient to squeeze at least a portionof the body 273, such as, but not limited to, along one or more sides273 b of the body 270 to release the one or more tabs 277 to allow thereservoir 280 to be inserted into or removed from the hollow interior275.

With reference to FIGS. 13-14B, in various embodiments, the transferguard 260 may include a body 265. The first needle 252 may be arrangedto pass through the body 265 to provide a fluid flow path between thevial 240 and the reservoir 280. In some embodiments, the body 265 may beformed by connecting the first end 262 and the second end 270 together(e.g., FIG. 13). In other embodiments, the body 265, the first end 262,and the second end 270 may be integral with each other (e.g., FIG. 14C).

In some embodiments, the transfer guard 260 may include an inner body250 located within the body 265. In such embodiments, the first needle252 may be arranged to pass through the body 265 and the inner body 250.The inner body 250 may be made of a material of suitable strength anddurability such as, but not limited to, plastic, metal, glass (e.g.,tempered glass), composite material, and/or the like. In someembodiments, the inner body 250 may be made of the same material as thebody 273 and/or the transfer guard 260 or a portion thereof. The innerbody 250 may be separate from or integrated with the body 265 of thetransfer guard 260.

The first needle 252 may have a first end 252 a (and/or opening alongthe first needle 252) and a second end 252 b (and/or opening along thefirst needle 252) opposite each other. The first end 252 a may be forarrangement in the vial 240, for example, in contact with fluidic mediain the interior volume 245 or the headspace 247 of the vial 240 in acase where the vial 240 is connected to the transfer guard 260. Thesecond end 252 b may be for arrangement in the reservoir 280, forexample, through the septum 284 into the port 282 of the reservoir 280.In some embodiments, one or more of the ends 252 a, 252 b of the firstneedle 252 may be beveled to provide one or more sharp ends to the firstneedle 252. In other embodiments, one or more of the ends 252 a, 252 bof the first needle 252 may be flat.

The second needle 256 may have a first end 256 a (and/or opening alongthe second needle 256) and a second end 256 b (and/or opening along thesecond needle 256) opposite each other. The first end 256 a may be forarrangement in the vial 240, for example, in contact with fluidic mediain the interior volume 245 or a headspace (e.g., 147 in FIG. 7) of thevial 240 in a case where the vial 240 is connected to the transfer guard260. The second end 256 b may be arranged in the transfer guard 260 orexternal to the transfer guard 260. In some embodiments, one or more ofthe ends 256 a, 256 b of the second needle 256 may be flat. In otherembodiments, one or more of the ends 256 a, 256 b of the second needle256 may be beveled to provide one or more sharp ends to the secondneedle 256.

In some embodiments, the inner body 250 may have a chamber 253. Infurther embodiments, the transfer guard 260 may include a mechanism toallow air to flow in one direction, such as, a valve 255 or a membrane,arranged within the chamber 253. The valve 255 may be, but is notlimited to, an umbrella valve, duckbill valve, ball check valve, or thelike.

The second end 256 b of the second needle 256 may be in communicationwith the chamber 253. The valve 255 may regulate flow of air into and/orout of the interior volume 245 of the vial 240 through the second needle256. Thus, the valve 255 may allow for equalizing pressure within theinterior volume 245 of the vial 240, for example, relative to atmosphereto facilitate transfer of fluidic media from the vial 240 to thereservoir 280. In yet further embodiments, the valve 255 may be providedwith a seal member 259 to prevent fluidic media from flowing past theseal member 259 and/or to facilitate movement of the valve 255 in thechamber 253. In some embodiments, one or more retaining members, such asridge 251, or the like, may be for retaining the valve 255 within thechamber 253.

In some embodiments, the valve 255 may have a channel 257 to allow thechamber 253 to communicate with atmosphere, for example, to allow air toflow into or out of the chamber 253. In some embodiments, the valve 255may substantially prevent liquid from coming out of the vial 240 throughthe second needle 256 and/or the valve 255. In various embodiments, thesecond needle 256 may allow for venting the headspace or the interiorvolume 245 of the vial 240 to atmosphere to facilitate the transfer offluidic media from the vial 240 to the reservoir 280. Thus, in suchembodiments, the valve 255 may allow pressure within the vial to beequalized or otherwise regulated to facilitate the transfer of fluidicmedia from the vial 240 to the reservoir 280.

In some embodiments, such as the embodiment exemplified in FIG. 14C, thesystem 200 may employ a transfer guard 260′, which may include featuressimilar to the transfer guard 260 (e.g., 9-14B). The transfer guard 260′may include a body 265′. A first needle 252′ may be arranged to passthrough the body 265′ to provide a fluid flow path between the vial 240and the reservoir 280. In some embodiments, the body 265′ may be formedby connecting the first end 262 and the second end 270 together (e.g.,FIG. 13). In other embodiments, the body 265′, the first end 262, andthe second end 270 may be integral with each other (e.g., FIG. 14C).

The first needle 252′ may have a first end 252 a′ (and/or opening alongthe first needle 252′) and a second end 252 b′ (and/or opening along thefirst needle 252′) opposite each other. The first end 252 a′ may be forarrangement in the vial 240, for example, in contact with fluidic mediain the interior volume 245 or the headspace 247 of the vial 240 in acase where the vial 240 is connected to the transfer guard 260′. Thesecond end 252 b′ may be for arrangement in the reservoir 280, forexample, through the septum 284 into the port 282 of the reservoir 280.In some embodiments, one or more of the ends 252 a′, 252 b′ of the firstneedle 252′ may be beveled to provide one or more sharp ends to thefirst needle 252′. In other embodiments, one or more of the ends 252 a′,252 b′ of the first needle 252′ may be flat.

At least a portion of the first needle 252′ may be arranged within atleast a portion of a second needle 256′. In some embodiments, the firstneedle 252′ (or at least a portion thereof) may be concentricallyarranged within the second needle 256′ (or at least a portion thereof).Thus in various embodiments, the first needle 252′ and the second needle256′ may share a common axis. In other embodiments, the first needle252′ (or at least a portion thereof) may be concentrically arrangedwithin the second needle 256′ (or at least a portion thereof) such thatthe first needle 252′ is offset from the second needle 256′ with aspacing 258. Thus in various embodiments, the first needle 252′ and thesecond needle 256′ each have their own axis parallel to each other.

In some embodiments, the transfer guard 260′ may have a chamber 253′.The chamber 253′ may be in communication with the interior volume 245 ofthe vial 240, for example, through the second needle 256′. For instance,one end 256 a′ (and/or opening) of the second needle 256′ may be incommunication with the interior volume 245 of the vial 240, and anotherend 256 b′ (and/or opening), opposite the end 256 a′, may be incommunication with the chamber 253′. In some embodiments, one or more ofthe ends 256 a′, 256 b′ of the second needle 256′ may be flat. In otherembodiments, one or more of the ends 256 a′, 256 b′ of the second needle256′ may be beveled to provide one or more sharp ends to the secondneedle 256′.

In further embodiments, the transfer guard 260′ may include a mechanismto allow air to flow in one direction, such as, a valve 255′ or amembrane, arranged within the chamber 253′. The valve 255′ may be, butis not limited to, an umbrella valve, duckbill valve, ball check valve,or the like.

The valve 255′ may regulate flow of air into and/or out of the interiorvolume 245 of the vial 240 through the needle 254′. Thus, the valve 255′may allow for equalizing pressure within the interior volume 245 of thevial 240, for example, relative to atmosphere to facilitate transfer offluidic media from the vial 240 to the reservoir 280. In yet furtherembodiments, the valve 255′ may be provided with a seal member (e.g.,259 in FIG. 14B) to prevent fluidic media from flowing past the sealmember and/or to facilitate movement of the valve 255′ in the chamber253′. In some embodiments, one or more retaining members, such as ridge(e.g., 251 in FIG. 14B), or the like, may be for retaining the valve255′ within the chamber 253′.

In some embodiments, the valve 255′ may have a channel 257′ to allow thechamber 253′ to communicate with atmosphere, for example, to allow airto flow into or out of the chamber 253′. In some embodiments, the valve255′ may substantially prevent liquid from coming out of the vial 240.In various embodiments, the second needle 256′ may allow for venting aheadspace (e.g., 147 in FIG. 7) or the interior volume 245 of the vial240 to atmosphere to facilitate the transfer of fluidic media from thevial 240 to the reservoir 280. Thus, in such embodiments, the valve 255′may allow pressure within the vial to be equalized or otherwiseregulated to facilitate the transfer of fluidic media from the vial 240to the reservoir 280.

Accordingly, in various embodiments, a second needle for equalizingpressure within a vial or to otherwise regulate or facilitate thetransfer of fluidic media from the vial to a reservoir may beconcentrically arranged around a first needle for transferring thefluidic media from the vial to the reservoir.

Referring to FIGS. 10 and 15 to operate the system 200, in step S1010,the vial 240 and the reservoir 280 may be attached or otherwise matedwith the first end 262 and the second end 270 of the transfer guard 260respectively. Then in step S1020, the plunger head 290 may be insertedinto the reservoir 280. Next in step S1030, the plunger arm 210 may beconnected to the plunger head 290 (if not integrated or alreadyconnected). In step S1040, the plunger arm casing 230 and reservoircover 234 may be arranged to support the plunger arm 210 and cover thereservoir 280. Then in step S1050, the handle 220 may be operativelyconnected to the plunger arm 210 as shown in FIG. 9.

With reference to FIGS. 9, 10, and 16A-17, the handle 220 may be foroperatively connecting to or otherwise engaging the plunger arm 210 toactuate or otherwise cause movement of the plunger arm 210 by advancingor withdrawing the handle 220 along line A. Because the plunger head 290may be attached to the plunger arm 210, movement of the handle 220 mayadvance or draw the plunger head 290 within the reservoir 280.Accordingly, fluidic media may be drawn from the vial 240 into thereservoir 280 by drawing the handle 290 and the operatively engagedplunger arm 210 and plunger head 290, for example, away from thereservoir 280.

The handle 220 may have a body 224 that may be sized and configured tocover at least a portion of the plunger arm casing 230. The body 224 mayhave an interior cavity 223 for receiving at least a portion of theplunger arm casing 230 within the interior cavity 223 through an opening223 a. The body 224 may be for supporting the plunger arm casing 230,for example, as the plunger arm 210 is moved along the plunger armcasing 230 and/or the reservoir 280. The body 224 may be made of amaterial of suitable strength and durability such as, but not limitedto, plastic, metal, glass (e.g., tempered glass), composite material,and/or the like. In some embodiments, the body 224 may be made of thesame material as the plunger arm casing 230.

At least one side of the plunger arm casing 230 may be in contact withone or more interior sides of the body 224. In some embodiments, thebody 224 may be for aligning the plunger arm casing 230 when the plungerarm casing 230 is placed within the interior cavity 223 of the body 224.In various embodiments, the plunger arm casing 230 may remainsubstantially still as the handle 220 actuates the plunger arm 210 alongthe plunger arm casing 230 and/or the reservoir 280.

The handle 220 may be configured to operatively engage and disengage theplunger arm 210 and/or the plunger arm casing 230 in any suitablemanner. In some embodiments, the handle 220 may have an engagementportion 226 for operatively engaging and disengaging the plunger arm210. Accordingly, movement of the handle 220 may actuate the plunger arm210 and therefore the plunger head 290 attached to the plunger arm 210to allow fluidic media to be drawn from the vial 240 to the reservoir280 via the first needle 252. The engagement portion 226 may have afirst end 226 a and a second end 226 b.

In some embodiments, a movable member, such as a slide 225, may bemounted on the engagement portion 226 and may be moveable at leastbetween the first end 226 a and the second end 226 b to lock and unlockthe handle 220 to the plunger arm 210. The first end 226 a and thesecond end 226 b may be for preventing the slide 225 from beingdismantled accidentally from the engagement portion 226. In someembodiments, the engagement portion 226 may include a rail 228 or thelike for allowing the slide 225 to slide or otherwise move at leastbetween the first end 226 a and the second end 226 b.

In other embodiments, the moveable member may be a rotatable member (notshown). The rotatable member may be moveable (e.g., rotatable) at leastbetween the first end 226 a and the second end 226 b to lock and unlockthe handle 220 to the plunger arm 210. For example, the rotatable membermay be rotatable about an axis of the handle 220. In other embodiments,the moveable member may be a hinged member (not shown) for locking andunlocking the handle 220 to the plunger arm 210.

In some embodiments, the engagement portion 226 may be pivotallymounted, cantilevered, biased, or otherwise positioned relative to thebody 224 of the handle 220. In such embodiments, the engagement portion226 may be adapted for pivotal movement about a pivot point 226 c. Theengagement portion 226 may include a member, such as a finger 227 or thelike, for engaging an aperture 211 or the like in the plunger arm 210.Accordingly, the finger 227 may be pivotable or otherwise moveabletoward and away from the body 224 as the engagement portion 226 ispivoted about the pivot point 226 c to engage and disengage the plungerarm 210.

In further embodiments, the engagement portion 226 may be pivoted aboutthe pivot point 226 c by movement of the slide 225. For example, bymoving the slide 225 toward the second end 226 b (e.g., FIG. 16A), afront portion of the engagement portion 226, which may include thefinger 227, may pivot upward. Accordingly, the plunger arm casing 230having the plunger arm 210 within may be placed at least partially inthe interior cavity 223 of the body 224. Then by moving the slide 225toward the first end 226 a (e.g., FIG. 9), the front portion of theengagement portion 226 and the finger 227 may pivot downward to allowthe finger 227 to engage the aperture 211 in the plunger arm 210, forexample, through the groove 238 in the plunge arm casing 230. The finger227 may remain engaged in the aperture 211 while the slide 225 remainsat or near the first end 226 a.

Once engaged, the handle 220 may be drawn away from the reservoir 240 todraw fluidic media from the vial 240 through the first needle 252 of thetransfer guard 260 to the reservoir 280. After the reservoir 280 issufficiently filled with a desired amount of fluidic media, the slide225 may be moved toward the second end 226 b to allow the front portionof the engagement portion 226 and the finger 227 to pivot upward todisengage the plunger arm 210. Accordingly, the user-patient may removethe reservoir 280, the plunger arm 210, and/or the plunger arm casing230 and insert the appropriate components in the delivery device (notshown) or provide another reservoir, plunger arm, and/or plunger armcasing in the system 200.

The handle 220 may include a base 222. The base 222 may be for standingthe system 200 vertically on a support surface. In some embodiments, thebase 222 may include an adhesive or the like for securing the handle 220to the support surface. Thus in some embodiments, in a case where thebase 222 of the system 200 on a support surface and fluidic media is tobe drawn from the vial 240 to the reservoir 280, the reservoir 280(along with the transfer guard 260 and the vial 240) may be drawn awayfrom the handle 220, which may remain substantially still, to transferfluidic media. In some embodiments, the base 222 may be for providingthe user-patient with a gripping area to use the system 200, forexample, to pull the handle 220 to draw fluidic media into the reservoir200.

Referring to FIGS. 9, 13, and 15, various embodiments of the system 200may allow for simplifying a filling process of the reservoir 280 withfluidic media from the vial 240. After step S1050, the handle 220operatively engaged with the plunger arm 210 may be pulled or otherwisemoved away from the reservoir 280. As the handle 220 moves away from thereservoir 280, the attached plunger arm 210 and plunger head 290 may bemoved within the reservoir 280 to increase the interior volume 285 ofthe reservoir 280. The movement of the plunger head 290 may draw fluidicmedia from the vial 240 through the first needle 252 of the transferguard 260 to the interior volume 285 of the reservoir 280 to transferfluidic media to the reservoir 280.

With reference to FIGS. 9-17, in various embodiments, the steps of theprocess 1000 may be performed in any suitable order. For example, thevial 240 may be attached to the transfer guard 260 after the handle 220is operatively engaged with the plunger arm 210. As another example, theplunger arm 210 may be connected to the plunger head 290 before theplunger head 290 is placed in the reservoir 280. In some embodiments,the plunger head 290 may be advanced within the reservoir 280 toward theport 282 of the reservoir 280 before starting the filling process of thereservoir 280, for example, to prime the system 200.

The system 200 may be used to fill the interior volume 285 of thereservoir 280, or a portion thereof. In some embodiments, the system 200may be configured such that the interior volume 285 of the reservoir 280is completely filled or sufficiently filled when the handle 290 is drawnas far from the reservoir 280 as the system allows.

The embodiments disclosed herein are to be considered in all respects asillustrative, and not restrictive of the invention. The presentinvention is in no way limited to the embodiments described above.Various modifications and changes may be made to the embodiments withoutdeparting from the spirit and scope of the invention. The scope of theinvention is indicated by the attached claims, rather than theembodiments. Various modifications and changes that come within themeaning and range of equivalency of the claims are intended to be withinthe scope of the invention.

1. A system for transferring fluidic media, the system comprising: asupport structure having a chamber, the support structure comprising: afirst adapter adapted to be mated to a vial having an interior volumecontaining fluidic media; and a second adapter adapted to be mated to areservoir having an interior volume for containing fluidic media and aplunger head arranged for movement within the reservoir; a first needlefor connecting the interior volume of the vial to the interior volume ofthe reservoir to provide a fluid flow path along a longitudinaldimension of the support structure from the interior volume of the vialto the interior volume of the reservoir; a second needle for connectingthe chamber and the interior volume of the vial; and an air flow controlmechanism arranged for movement within the chamber along thelongitudinal dimension of the support structure to selectively allow airto flow in one direction in a case where the second needle connects thechamber and the vial and the plunger head is moved within the reservoirto transfer fluidic media through the fluid flow path from the interiorvolume of the vial to the interior volume of the reservoir.
 2. Thesystem of claim 1, the air flow control mechanism adapted to allow thechamber to communicate with atmosphere to equalize pressure relative toatmosphere in the interior volume of the vial in a case where the secondneedle connects the chamber and the vial and the plunger head is movedwithin the reservoir to transfer fluidic media from the interior volumeof the vial to the interior volume of the reservoir.
 3. The system ofclaim 1, wherein at least a portion of the first needle isconcentrically arranged within at least a portion of the second needle.4. The system of claim 3, wherein the first needle and the second needleshare a common axis.
 5. The system of claim 3, wherein an axis of thefirst needle and an axis of the second needle are parallel to eachother; and wherein the axis of the first needle is offset from the axisof the second needle.
 6. The system of claim 1, wherein the air flowcontrol mechanism comprises a valve.
 7. The system of claim 6, whereinthe air flow control mechanism comprises at least one of an umbrellavalve and a duckbill valve.
 8. The system of claim 6, the valve moveableat least between a first position and a second position; the chamber forcommunicating with atmosphere in a case where the valve is in the secondposition and the fluid flow path is established.
 9. The system of claim1, the second adapter comprising a body configured to envelop thereservoir.
 10. The system of claim 9, the body adapted to allow fluidicmedia in the reservoir to be viewable through the body in a case wherethe reservoir is connected to the second adapter and the reservoircontains fluidic media.
 11. The system of claim 10, the body having anopening for allowing fluidic media in the reservoir to be viewable andfor allowing a user-patient to provide further support to the reservoirduring use of the system.
 12. The system of claim 9, the body having oneor more fill lines for measuring a volume of fluidic media in thereservoir.
 13. The system of claim 1, wherein the airflow controlmechanism is enclosed completely within the chamber.
 14. The system ofclaim 13, the airflow control mechanism having a longitudinal dimensionparallel with the longitudinal dimension of the support structure; theairflow control mechanism having a first surface opposite a secondsurface, the first surface and the second surface aligned along thelongitudinal dimension of the airflow control mechanism; wherein thefirst surface faces the reservoir when the reservoir is mated with thesecond adapter.
 15. The system of claim 1, wherein the airflow controlmechanism includes a body having a channel extending through the body,the channel for communicating between the chamber and atmosphere. 16.The system of claim 1, wherein the air flow control mechanism isarranged for movement in a same direction as a direction in which fluidis transferred from the vial to the reservoir.
 17. The system of claim1, wherein the air flow control mechanism is arranged for movement in adirection toward the reservoir.
 18. A method of making a system fortransferring fluidic media, the method comprising: supporting a supportstructure having a chamber, the support structure comprising: a firstadapter adapted to be mated to a vial having an interior volumecontaining fluidic media; and a second adapter adapted to be mated to areservoir having an interior volume for containing fluidic media and aplunger head arranged for movement within the reservoir; connecting theinterior volume of the vial to the interior volume of the reservoir toprovide a fluid flow path along a longitudinal dimension of the supportstructure from the interior volume of the vial to the interior volume ofthe reservoir with a first needle; connecting the chamber and theinterior volume of the vial with a second needle; and arranging an airflow control mechanism for movement within the chamber along thelongitudinal dimension of the support structure the mechanism toselectively allow air to flow in one direction to communicate withatmosphere in a case where the second needle connects the chamber andthe vial and the plunger head is moved within the reservoir to transferfluidic media through the fluid flow path from the interior volume ofthe vial to the interior volume of the reservoir.
 19. The method ofclaim 18, further comprising adapting the air flow control mechanism toallow the chamber to communicate with atmosphere to equalize pressurerelative to atmosphere in the interior volume of the vial in a casewhere the second needle connects the chamber and the vial and theplunger head is moved within the reservoir to transfer fluidic mediafrom the interior volume of the vial to the interior volume of thereservoir.
 20. The method of claim 18, further comprising concentricallyarranging at least a portion of the first needle within at least aportion of the second needle.
 21. The method of claim 18, wherein thefirst needle and the second needle share a common axis.
 22. The methodof claim 18, wherein an axis of the first needle and an axis of thesecond needle are parallel to each other; and wherein the axis of thefirst needle is offset from the axis of the second needle.
 23. Themethod of claim 18, the second adapter comprising a body, the methodfurther comprising enveloping the reservoir with the body of the secondadapter.
 24. The method of claim 18, further comprising configuring thebody to allow fluidic media in the reservoir to be viewable through thebody in a case where the reservoir is connected to the second adapterand the reservoir contains fluidic media.